A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1031147



Internal ID19120368
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:67346326..67457363hg38UCSC Ensembl
Innerchr7:66811313..66922350hg19UCSC Ensembl
Innerchr7:66448748..66559785hg18UCSC Ensembl
Cytoband7q11.21
Allele length
AssemblyAllele length
hg38111038
hg19111038
hg18111038
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3655631
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1031147
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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